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Serotonin and dopamine modulate aging in response to food odor and availability

An organism’s ability to perceive and respond to changes in its environment is crucial for its health and survival. Here we reveal how the most well-studied longevity intervention, dietary restriction, acts in-part through a cell non-autonomous signaling pathway that is inhibited by the presence of...

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Autores principales: Miller, Hillary A., Huang, Shijiao, Dean, Elizabeth S., Schaller, Megan L., Tuckowski, Angela M., Munneke, Allyson S., Beydoun, Safa, Pletcher, Scott D., Leiser, Scott F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174215/
https://www.ncbi.nlm.nih.gov/pubmed/35672307
http://dx.doi.org/10.1038/s41467-022-30869-5
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author Miller, Hillary A.
Huang, Shijiao
Dean, Elizabeth S.
Schaller, Megan L.
Tuckowski, Angela M.
Munneke, Allyson S.
Beydoun, Safa
Pletcher, Scott D.
Leiser, Scott F.
author_facet Miller, Hillary A.
Huang, Shijiao
Dean, Elizabeth S.
Schaller, Megan L.
Tuckowski, Angela M.
Munneke, Allyson S.
Beydoun, Safa
Pletcher, Scott D.
Leiser, Scott F.
author_sort Miller, Hillary A.
collection PubMed
description An organism’s ability to perceive and respond to changes in its environment is crucial for its health and survival. Here we reveal how the most well-studied longevity intervention, dietary restriction, acts in-part through a cell non-autonomous signaling pathway that is inhibited by the presence of attractive smells. Using an intestinal reporter for a key gene induced by dietary restriction but suppressed by attractive smells, we identify three compounds that block food odor effects in C. elegans, thereby increasing longevity as dietary restriction mimetics. These compounds clearly implicate serotonin and dopamine in limiting lifespan in response to food odor. We further identify a chemosensory neuron that likely perceives food odor, an enteric neuron that signals through the serotonin receptor 5-HT1A/SER-4, and a dopaminergic neuron that signals through the dopamine receptor DRD2/DOP-3. Aspects of this pathway are conserved in D. melanogaster. Thus, blocking food odor signaling through antagonism of serotonin or dopamine receptors is a plausible approach to mimic the benefits of dietary restriction.
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spelling pubmed-91742152022-06-09 Serotonin and dopamine modulate aging in response to food odor and availability Miller, Hillary A. Huang, Shijiao Dean, Elizabeth S. Schaller, Megan L. Tuckowski, Angela M. Munneke, Allyson S. Beydoun, Safa Pletcher, Scott D. Leiser, Scott F. Nat Commun Article An organism’s ability to perceive and respond to changes in its environment is crucial for its health and survival. Here we reveal how the most well-studied longevity intervention, dietary restriction, acts in-part through a cell non-autonomous signaling pathway that is inhibited by the presence of attractive smells. Using an intestinal reporter for a key gene induced by dietary restriction but suppressed by attractive smells, we identify three compounds that block food odor effects in C. elegans, thereby increasing longevity as dietary restriction mimetics. These compounds clearly implicate serotonin and dopamine in limiting lifespan in response to food odor. We further identify a chemosensory neuron that likely perceives food odor, an enteric neuron that signals through the serotonin receptor 5-HT1A/SER-4, and a dopaminergic neuron that signals through the dopamine receptor DRD2/DOP-3. Aspects of this pathway are conserved in D. melanogaster. Thus, blocking food odor signaling through antagonism of serotonin or dopamine receptors is a plausible approach to mimic the benefits of dietary restriction. Nature Publishing Group UK 2022-06-07 /pmc/articles/PMC9174215/ /pubmed/35672307 http://dx.doi.org/10.1038/s41467-022-30869-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Miller, Hillary A.
Huang, Shijiao
Dean, Elizabeth S.
Schaller, Megan L.
Tuckowski, Angela M.
Munneke, Allyson S.
Beydoun, Safa
Pletcher, Scott D.
Leiser, Scott F.
Serotonin and dopamine modulate aging in response to food odor and availability
title Serotonin and dopamine modulate aging in response to food odor and availability
title_full Serotonin and dopamine modulate aging in response to food odor and availability
title_fullStr Serotonin and dopamine modulate aging in response to food odor and availability
title_full_unstemmed Serotonin and dopamine modulate aging in response to food odor and availability
title_short Serotonin and dopamine modulate aging in response to food odor and availability
title_sort serotonin and dopamine modulate aging in response to food odor and availability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174215/
https://www.ncbi.nlm.nih.gov/pubmed/35672307
http://dx.doi.org/10.1038/s41467-022-30869-5
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